Inflammatory profile discriminates clinical subtypes in LRRK2‐associated Parkinson's disease
Brockmann, K., Schulte, C., Schneiderhan‐Marra, N., Apel, A., Pont‐Sunyer, C., Vilas, D., Ruiz‐Martinez, J., Langkamp, M., Corvol, J.‐C., Cormier, F., Knorpp, T., Joos, T. O., Bernard, A., Gasser, T., Marras, C., Schüle, B., Aasly, J. O., Foroud, T., Marti‐Masso, J. F., Brice, A., Tolosa, E., Berg, D., Maetzler, W.
Published in European journal of neurology (01.02.2017)
Published in European journal of neurology (01.02.2017)
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Cerebrospinal fluid amyloid β and tau in LRRK2 mutation carriers
Aasly, J O, Shi, M, Sossi, V, Stewart, T, Johansen, K K, Wszolek, Z K, Uitti, R J, Hasegawa, K, Yokoyama, T, Zabetian, C P, Kim, H M, Leverenz, J B, Ginghina, C, Armaly, J, Edwards, K L, Snapinn, K W, Stoessl, A J, Zhang, J
Published in Neurology (03.01.2012)
Published in Neurology (03.01.2012)
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Parkinson-related genetics in patients treated with deep brain stimulation
Johansen, K. K., Jørgensen, J. V., White, L. R., Farrer, M. J., Aasly, J. O.
Published in Acta neurologica Scandinavica (01.03.2011)
Published in Acta neurologica Scandinavica (01.03.2011)
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Characterization of DCTN1 genetic variability in neurodegeneration
Vilariño-Güell, C, Wider, C, Soto-Ortolaza, A I, Cobb, S A, Kachergus, J M, Keeling, B H, Dachsel, J C, Hulihan, M M, Dickson, D W, Wszolek, Z K, Uitti, R J, Graff-Radford, N R, Boeve, B F, Josephs, K A, Miller, B, Boylan, K B, Gwinn, K, Adler, C H, Aasly, J O, Hentati, F, Destée, A, Krygowska-Wajs, A, Chartier-Harlin, M-C, Ross, O A, Rademakers, R, Farrer, M J
Published in Neurology (09.06.2009)
Published in Neurology (09.06.2009)
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PINK1 mutation heterozygosity and the risk of Parkinson’s disease
Toft, M, Myhre, R, Pielsticker, L, White, L R, Aasly, J O, Farrer, M J
Published in Journal of neurology, neurosurgery and psychiatry (01.01.2007)
Published in Journal of neurology, neurosurgery and psychiatry (01.01.2007)
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An independent replication of PARK16 in Asian samples
Vilariño-Güell, C, Ross, O A, Aasly, J O, White, L R, Rajput, A, Rajput, A H, Lynch, T, Krygowska-Wajs, A, Jasinska-Myga, B, Opala, G, Barcikowska, M, Lee, M-C, Hentati, F, Uitti, R J, Wszolek, Z K, Farrer, M J, Wu, R-M
Published in Neurology (14.12.2010)
Published in Neurology (14.12.2010)
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MEIS1 p.R272H in familial restless legs syndrome
Vilariño-Güell, C, Chai, H, Keeling, B H, Young, J E, Rajput, A, Lynch, T, Aasly, J O, Uitti, R J, Wszolek, Z K, Farrer, M J, Lin, S-C
Published in Neurology (21.07.2009)
Published in Neurology (21.07.2009)
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Association of the MAPT locus with Parkinson's disease
Wider, C., Vilariño-Güell, C., Jasinska-Myga, B., Heckman, M. G., Soto-Ortolaza, A. I., Cobb, S. A., Aasly, J. O., Gibson, J. M., Lynch, T., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.
Published in European journal of neurology (01.03.2010)
Published in European journal of neurology (01.03.2010)
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SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction study
Wider, C., Vilariño-Güell, C., Heckman, M. G., Jasinska-Myga, B., Ortolaza-Soto, A. I., Diehl, N. N., Crook, J. E., Cobb, S. A., Bacon, J. A., Aasly, J. O., Gibson, J. M., Lynch, T., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.
Published in European journal of neurology (01.06.2011)
Published in European journal of neurology (01.06.2011)
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Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
Sidransky, E, Nalls, M.A, Aasly, J.O, Aharon-Peretz, J, Annesi, G, Barbosa, E.R, Bar-Shira, A, Berg, D, Bras, J, Brice, A, Chen, C.-M, Clark, L.N, Condroyer, C, De Marco, E.V, Dürr, A, Eblan, M.J, Fahn, S, Farrer, M.J, Fung, H.-C, Gan-Or, Z, Gasser, T, Gershoni-Baruch, R, Giladi, N, Griffith, A, Gurevich, T, Januario, C, Kropp, P, Lang, A.E, Lee-Chen, G.-J, Lesage, S, Marder, K, Mata, I.F, Mirelman, A, Mitsui, J, Mizuta, I, Nicoletti, G, Oliveira, C, Ottman, R, Orr-Urtreger, A, Pereira, L.V, Quattrone, A, Rogaeva, E, Rolfs, A, Rosenbaum, H, Rozenberg, R, Samii, A, Samaddar, T, Schulte, C, Sharma, M, Singleton, A, Spitz, M, Tan, E.-K, Tayebi, N, Toda, T, Troiano, A.R, Tsuji, S, Wittstock, M, Wolfsberg, T.G, Wu, Y.-R, Zabetian, C.P, Zhao, Y, Ziegler, S.G
Published in The New England journal of medicine (22.10.2009)
Published in The New England journal of medicine (22.10.2009)
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Death-associated protein kinase 1 variation and Parkinson's disease
Dachsel, J. C., Wider, C., Vilariño-Güell, C., Aasly, J. O., Rajput, A., Rajput, A. H., Lynch, T., Craig, D., Krygowska-Wajs, A., Jasinska-Myga, B., Opala, G., Barcikowska, M., Czyzewski, K., Wu, R. -M., Heckman, M. G., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.
Published in European journal of neurology (01.08.2011)
Published in European journal of neurology (01.08.2011)
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Calbindin-1 association and Parkinson's disease
Soto-Ortolaza, A. I., Behrouz, B., Wider, C., Vilariño-Güell, C., Heckman, M. G., Aasly, J. O., Mark Gibson, J., Lynch, T., Jasinska-Myga, B., Krygowska-Wajs, A., Opala, G., Barcikowska, M., Czyzewski, K., Uitti, R. J., Wszolek, Z. K., Farrer, M. J., Ross, O. A.
Published in European journal of neurology (01.02.2010)
Published in European journal of neurology (01.02.2010)
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LRRK2 and Parkinson's disease in Norway
Toft, M., Haugarvoll, K., Ross, O. A., Farrer, M. J., Aasly, J. O.
Published in Acta neurologica Scandinavica (01.05.2007)
Published in Acta neurologica Scandinavica (01.05.2007)
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Clinical features of LRRK2-associated Parkinson's disease in central Norway
Aasly, Jan O., Toft, Mathias, Fernandez-Mata, Ignacio, Kachergus, Jennifer, Hulihan, Mary, White, Linda R., Farrer, Matthew
Published in Annals of neurology (01.05.2005)
Published in Annals of neurology (01.05.2005)
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A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants (vol 49, pg 721, 2012)
Sharma, M, Ioannidis, JP, Aasly, JO, Annesi, G, Brice, A, Bertram, L, Bozi, M, Barcikowska, M, Crosiers, D, Clarke, CE, Facheris, MF, Farrer, M, Garraux, G, Gispert, S, Auburger, G, Vilarino-Guell, C, Hadjigeorgiou, GM, Hicks, AA, Hattori, N, Jeon, BS, Jamrozik, Z, Krygowska-Wajs, A, Lesage, S, Lill, CM, Lin, JJ, Lynch, T, Lichtner, P, Lang, AE, Libioulle, C, Murata, M, Mok, V, Jasinska-Myga, B, Mellick, GD, Morrison, KE, Meitnger, T, Zimprich, A, Opala, G, Pramstaller, PP, Pichler, I, Park, SS, Quattrone, A, Rogaeva, E, Ross, OA, Stefanis, L, Stockton, JD, Satake, W, Silburn, PA, Strom, TM, Theuns, J, Tan, EK, Toda, T, Tomiyama, H, Uitti, RJ, Van Broeckhoven, C, Wirdefeldt, K, Wszolek, Z, Xiromerisiou, G, Yomono, HS, Yueh, KC, Zhao, Y, Gasser, T, Maraganore, D, Kruger, R
Published in Journal of medical genetics (01.03.2013)
Published in Journal of medical genetics (01.03.2013)
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